期刊
EUROPEAN JOURNAL OF MASS SPECTROMETRY
卷 18, 期 2, 页码 235-250出版社
SAGE PUBLICATIONS LTD
DOI: 10.1255/ejms.1177
关键词
IRMPD sSpectroscopy; metal cation; DNA base; FT-ICR; mass spectrometry; electronic structure calculations; amino acids; gas phase; solvation
资金
- National Sciences and Engineering Research Council (NSERC)
- Canadian Foundation for Innovation (CFI)
Metal chelation can alter the activity of free biomolecules by modifying their structures or stabilizing higher energy tautomers. In recent years, mass spectrometric techniques have been used to investigate the effects of metal complexation with proteins, nucleobases and nucleotides, where small conformational changes can have significant physiological consequences. In particular, infrared multiple photon dissociation spectroscopy has emerged as an important tool for determining the structure and reactivity of gas-phase ions. Unlike other mass spectrometric approaches, this method is able to directly resolve structural isomers using characteristic vibrational signatures. Other activation and dissociation methods, such as blackbody infrared radiative dissociation or collision-induced dissociation can also reveal information about the thermochemistry and dissociative pathways of these biological ions. This information can then be used to provide information about the structures of the ionic complexes under study. In this article, we review the use of gas-phase techniques in characterizing metal-bound biomolecules. Particular attention will be given to our own contributions, which detail the ability of metal cations to disrupt nucleobase pairs, direct the self-assembly of nucleobase clusters and stabilize non-canonical isomers of amino acids.
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